Overlap Molecular QTLs

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library(workflowr)

This is workflowr version 1.1.1
Run ?workflowr for help getting started

library(reshape2)
library(tidyverse)

── Attaching packages ──────────────────────────────────────────────────────── tidyverse 1.2.1 ──

✔ ggplot2 3.0.0     ✔ purrr   0.2.5
✔ tibble  1.4.2     ✔ dplyr   0.7.6
✔ tidyr   0.8.1     ✔ stringr 1.3.1
✔ readr   1.1.1     ✔ forcats 0.3.0

── Conflicts ─────────────────────────────────────────────────────────── tidyverse_conflicts() ──
✖ dplyr::filter() masks stats::filter()
✖ dplyr::lag()    masks stats::lag()

library(VennDiagram)

Loading required package: grid

Loading required package: futile.logger

Permuted Results from APA:

nuclearAPA=read.table("../data/perm_QTL_trans/filtered_APApeaks_merged_allchrom_refseqGenes_pheno_Nuclear_transcript_permResBH.txt", stringsAsFactors = F, header = T)
totalAPA=read.table("../data/perm_QTL_trans/filtered_APApeaks_merged_allchrom_refseqGenes_pheno_Total_transcript_permResBH.txt", stringsAsFactors = F, header=T)  

Permuted results for other QTLs

perm_names=c("pid" ,"nvar","shape1" ,"shape2", "dummy","sid" ,"dist","npval", "slope" , "ppval" ,"bpval")
su30=read.table("../data/other_qtls/fastqtl_qqnorm_4su30.fixed.perm.out", stringsAsFactors = F,col.names = perm_names)
su60=read.table("../data/other_qtls/fastqtl_qqnorm_4su60.fixed.perm.out", stringsAsFactors = F,col.names = perm_names)

rna=read.table("../data/other_qtls/fastqtl_qqnorm_RNAseq_phase2.fixed.perm.out", stringsAsFactors = F,col.names = perm_names)
rib=read.table("../data/other_qtls/fastqtl_qqnorm_ribo_phase2.fixed.perm.out", stringsAsFactors = F,col.names = perm_names)
prot=read.table("../data/other_qtls/fastqtl_qqnorm_prot.fixed.perm.out", stringsAsFactors = F,col.names = perm_names)

Create overlap plot

I will write this in multiple functions and put them together. The first function will take in the permuted results and return the significant snps at a given FDR.

First step is to take in the mol file and change the names:

geneNames=read.table("/project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt", sep="\t", header=T,stringsAsFactors = F)
 
file_newNames=mol_file %>% separate(pid, into=c("Gene.stable.ID", "ver"), sep ="[.]") %>% inner_join(geneNames, by="Gene.stable.ID") %>% dplyr::select("Gene.name", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval")

#returns significant snps given a file and a cutoff 
sigsnp=function(file, cutoff){
  file$bh=p.adjust(file$bpval, method="fdr")
  file_sig=file %>% filter(-log10(bh)> cutoff) %>% select(Gene.name, sid)
  return(file_sig)
}

testsigsnp=sigsnp(rna,1 )

Next step is to choose a random subset with the same number of snps as were found significant.

#takes the file and the list of sig snps, returns a df with the same number of random snps  
randomsnps=function(file, SigSnpList){
  nsnp=nrow(SigSnpList)
  randomSnpDF= file %>% sample_n(nsnp) %>% arrange(sid) %>% select(Gene.name,sid) 
  return(randomSnpDF)
}
testrandomsnps=randomsnps(rna, testsigsnp)

The next step is to filter nuclear file by the snp id and gene. To do this I will join on the snpIDs then group by the snp ids. I should then be able to take the lowest Pvalue from each group and count how many are in each group to multiply by the number of tests. I will practice this with a small set then make the general function.

#filter and fix pvals
filt_tot= totalAPA %>% semi_join(testrandomsnps, by=c("Gene.name","sid") %>% group_by(sid) %>% add_tally() %>% ungroup() %>% mutate(corrPval=bpval * n)
#take top snp
filt_tot_top= filt_tot %>% group_by(sid) %>% top_n(-1, corrPval)

Make this into a function for the total and nuclear:

nom_names=c("peakID", "sid", "dist", "pval", "slope")
#import total nominal
apaTotNom=read_table("/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes_pheno_Total_NomRes.txt", col_names=nom_name, col_types = c(col_character(), col_character(), col_double(), col_double(), col_double()))
#import nuclear nominal
apaNucNom=read_table("/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes_pheno_Nuclear_NomRes.txt", col_names=nom_name, col_types = nom_names c(col_character(), col_character(), col_double(), col_double(), col_double()))


#takes a list of snps and filters the top corrected snp for each one, returns df
top_Total=function(snp_list){
  filt_tot=apaTotNom %>% separate(peakID, into=c("chr", "start", "end", "id"), sep=":") %>% separate(id, into=c("Gene.name", "strand", "peaknum"), sep="_") %>% semi_join(snp_list, by=c("sid", "Gene.name") %>% group_by(sid, Gene.name) %>% add_tally() %>% ungroup() %>% mutate(corrPval=bpval* n)
  filt_tot_top= filt_tot %>% group_by(sid, Gene.name) %>% top_n(-1, corrPval)
  return(filt_tot_top)
}

#same for nuclear:  
top_Nuclear=function(snp_list){
  filt_nuc=apaNucNom  %>% separate(peakID, into=c("chr", "start", "end", "id"), sep=":") %>% separate(id, into=c("Gene.name", "strand", "peaknum"), sep="_") %>% semi_join(snp_list, by=c("sid", "Gene.name") %>% group_by(sid, Gene.name) %>% add_tally() %>% ungroup() %>% mutate(corrPval=bpval* n)
  filt_nuc_top= filt_nuc %>% group_by(sid, Gene.name) %>% top_n(-1, corrPval)
  return(filt_nuc_top)
}

In the full script I will run this on the real QTLs and the random snps.

The next function will make the plots. I will make one that takes the results of the top_total or top_Nuclear snps.

#function returns a QQplot when given the results of the top_X functions. One will be the test set (real QTLs) and 1 will be the baseline snps.

makeQQ=function(test, baseline, Mol, Fraction){
  plot=qqplot(-log10(runif(nrow(baseline))), -log10(baseline$corrPval), ylab="Observed", xlab="Expected", main=paste("Overlap QTLs:", Mol, "with APA", Fraction, sep=" "))
  points(sort(-log10(runif(nrow(test)))), sort(-log10(test$corrPval)), col= alpha("Red"))
  abline(0,1)
  return(plot)
}

Put these together in a function: I want to give the function the molQTL file and it will make the total and nuclear plots. This means I need to give it the file to write the png files to.

createOverlapSigMol2APA.R

#!/bin/rscripts

#this script creates the files for the molQTLs overlap with total and nuclear APA qtl

library(dplyr)
library(tidyr)
library(ggplot2)
library(readr)
library(optparse)

#this script will take the total and nuclear nominal file for a given, then output files to put the total/nuclear/base/test files into, and the mol QTL permuted results 
option_list = list(
    make_option(c("-T", "--file_Total"), action="store", default=NA, type='character',
              help="input nom file total"),
    make_option(c("-N", "--file_Nuclear"), action="store", default=NA, type='character',
              help="input nom file nuclear"),
    make_option(c("-A", "--output_test_total"), action="store", default=NA, type='character', help="output for test set total"),
    make_option(c("-B", "--output_test_nuclear"), action="store", default=NA, type='character', help="output for test set nulear"),
        make_option(c("-C", "--output_base_total"), action="store", default=NA, type='character', help="output for base total"),
            make_option(c("-D", "--output_base_nuclear"), action="store", default=NA, type='character', help="output for baseset nuclear"),
            make_option(c("-M", "--molPhenoQTLperm"), action="store", default=NA, type='character', help="permuter results for molecular pheno")
)


opt_parser <- OptionParser(option_list=option_list)
opt <- parse_args(opt_parser)
print(opt)

nom_name=c("peakID", "sid", "dist", "pval", "slope")


geneNames=read.table("/project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt", sep="\t", header=T, stringsAsFactors = F)


#function to run per mol QTLs

overlapQTLplot=function(mol_file, cut, optA=opt, nom_nameA=nom_name){

if (mol_file == "/project2/gilad/briana/threeprimeseq/data/molecular_QTLs/perm/fastqtl_qqnorm_prot.fixed.perm.out") {
  in_file=read.table(mol_file, col.names = c("Gene.stable.ID", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval"),stringsAsFactors=F)
  file_newNames=in_file %>%  inner_join(geneNames, by="Gene.stable.ID") %>% dplyr::select("Gene.name", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval")
} else {
in_file=read.table(mol_file, col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval"),stringsAsFactors=F)
file_newNames=in_file %>% separate(pid, into=c("Gene.stable.ID", "ver"), sep ="[.]") %>% inner_join(geneNames, by="Gene.stable.ID") %>% dplyr::select("Gene.name", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval")
}
  
    #helper functions  
#returns significant snps given a file and a cutoff 
  sigsnp=function(file, cutoff){
    file$bh=p.adjust(file$bpval, method="fdr")
    file_sig=file %>% filter(-log10(bh)> cutoff) %>% select(Gene.name, sid)
    return(file_sig)
  }
  randomsnps=function(file, SigSnpList){
    nsnp=nrow(SigSnpList)
    randomSnpDF= file %>% sample_n(nsnp) %>% arrange(sid) %>% select(Gene.name,sid) 
    return(randomSnpDF)
  }

#takes a list of snps and filters the top corrected snp for each one, returns df
    top_Total=function(snp_list,optB=optA,nom_name1=nom_nameA){
      apaTotNom=read.table(optB$file_Total, col.names=nom_name1,stringsAsFactors=F)
      filt_tot=apaTotNom %>% separate(peakID, into=c("chr", "start", "end", "id"), sep=":") %>% separate(id, into=c("Gene.name", "strand", "peaknum"), sep="_") %>% semi_join(snp_list, by=c("sid", "Gene.name")) %>% group_by(sid, Gene.name) %>% add_tally() %>% ungroup() %>% mutate(corrPval= pval * n)
      filt_tot_top= filt_tot %>% group_by(sid, Gene.name) %>% top_n(-1, corrPval)
      return(as.data.frame(filt_tot_top))
    }
    #same for nuclear:  
    top_Nuclear=function(snp_list,optC=optA, nom_name2=nom_nameA){
      apaNucNom=read.table(optC$file_Nuclear, col.names=nom_name2,stringsAsFactors=F)
      filt_nuc=apaNucNom  %>% separate(peakID, into=c("chr", "start", "end", "id"), sep=":") %>% separate(id, into=c("Gene.name", "strand", "peaknum"), sep="_") %>% semi_join(snp_list, by=c("sid", "Gene.name")) %>% group_by(sid, Gene.name) %>% add_tally() %>% ungroup() %>% mutate(corrPval=pval* n)
      filt_nuc_top= filt_nuc %>% group_by(sid, Gene.name) %>% top_n(-1, corrPval)
      return(as.data.frame(filt_nuc_top))
    }
    TL=sigsnp(file_newNames, cut)
    BL=randomsnps(file_newNames, TL)
    #top snps test and base total
    topT_T=top_Total(TL)
    topT_B=top_Total(BL)
    
    #top snps test and base total
    topN_T=top_Nuclear(TL)
    topN_B=top_Nuclear(BL)
    return(list(TT=topT_T,TB=topT_B, NT=topN_T,NB=topN_B))

}
 
outputFiles=overlapQTLplot(opt$molPhenoQTLperm, 1)

#write tables 
write.table(outputFiles$TT,opt$output_test_total,quote=F,row.names = F, col.names=T )
write.table(outputFiles$TB,opt$output_base_total,quote=F,row.names = F, col.names=T )
write.table(outputFiles$NT,opt$output_test_nuclear,quote=F,row.names = F, col.names=T )
write.table(outputFiles$NB,opt$output_base_nuclear,quote=F,row.names = F, col.names=T )

maybe try as.data.frame

Directories for output:

Run this on chr 13, protein:

test_createOverlapSigMol2APA.sh

#!/bin/bash


#SBATCH --job-name=test_createOverlapSigMol2APA
#SBATCH --account=pi-yangili1
#SBATCH --time=24:00:00
#SBATCH --output=test_createOverlapSigMol2APA.out
#SBATCH --error=test_createOverlapSigMol2APA.err
#SBATCH --partition=bigmem2
#SBATCH --mem=64G
#SBATCH --mail-type=END


module load R


Rscript createOverlapSigMol2APA.R --file_Total "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Total.pheno_fixed.txt.gz.qqnorm_chr13.nominal.out" --file_Nuclear "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Nuclear.pheno_fixed.txt.gz.qqnorm_chr13.nominal.out" --output_test_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigProteinQTL_overlapAPA_Total.test.chr13.txt" --output_test_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigProteinQTL_overlapAPA_Nuclear.test.chr13.txt" --output_base_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigProteinQTL_overlapAPA_Total.base.chr13.txt" --output_base_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigProteinQTL_overlapAPA_Nuclear.base.chr13.txt" --molPhenoQTLperm "/project2/gilad/briana/threeprimeseq/data/molecular_QTLs/perm/fastqtl_qqnorm_prot.fixed.perm.out"

Run this on all individuals and all phenos:

run_createOverlapSigMol2APA_prot.sh

#!/bin/bash


#SBATCH --job-name=run_createOverlapSigMol2APA_prot
#SBATCH --account=pi-yangili1
#SBATCH --time=24:00:00
#SBATCH --output=run_createOverlapSigMol2APA_prot.out
#SBATCH --error=run_createOverlapSigMol2APA_prot.err
#SBATCH --partition=bigmem2
#SBATCH --mem=64G
#SBATCH --mail-type=END


module load R

#protein 
for i in $(seq 1 22)
do
Rscript createOverlapSigMol2APA.R --file_Total "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Total.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --file_Nuclear "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Nuclear.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --output_test_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigProteinQTL_overlapAPA_Total.test.chr${i}.txt" --output_test_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigProteinQTL_overlapAPA_Nuclear.test.chr${i}.txt" --output_base_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigProteinQTL_overlapAPA_Total.base.chr${i}.txt" --output_base_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigProteinQTL_overlapAPA_Nuclear.base.chr${i}.txt"  --molPhenoQTLperm "/project2/gilad/briana/threeprimeseq/data/molecular_QTLs/perm/fastqtl_qqnorm_prot.fixed.perm.out"
done 

run_createOverlapSigMol2APA_4su30.sh

#!/bin/bash


#SBATCH --job-name=run_createOverlapSigMol2APA_4su30
#SBATCH --account=pi-yangili1
#SBATCH --time=24:00:00
#SBATCH --output=run_createOverlapSigMol2APA_4su30.out
#SBATCH --error=run_createOverlapSigMol2APA_4su30.err
#SBATCH --partition=bigmem2
#SBATCH --mem=64G
#SBATCH --mail-type=END


module load R
#4su30
for i in $(seq 1 22)
do
Rscript createOverlapSigMol2APA.R --file_Total "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Total.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --file_Nuclear "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Nuclear.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --output_test_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/Sig4su30QTL_overlapAPA_Total.test.chr${i}.txt" --output_test_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/Sig4su30QTL_overlapAPA_Nuclear.test.chr${i}.txt" --output_base_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/Sig4su30QTL_overlapAPA_Total.base.chr${i}.txt" --output_base_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/Sig4su30QTL_overlapAPA_Nuclear.base.chr${i}.txt"  --molPhenoQTLperm "/project2/gilad/briana/threeprimeseq/data/molecular_QTLs/perm/fastqtl_qqnorm_4su30.fixed.perm.out"
done 

run_createOverlapSigMol2APA_4su60.sh

#!/bin/bash


#SBATCH --job-name=run_createOverlapSigMol2APA_4su60
#SBATCH --account=pi-yangili1
#SBATCH --time=24:00:00
#SBATCH --output=run_createOverlapSigMol2APA_4su60.out
#SBATCH --error=run_createOverlapSigMol2APA_4su60.err
#SBATCH --partition=bigmem2
#SBATCH --mem=64G
#SBATCH --mail-type=END


module load R
#4su60
for i in $(seq 1 22)
do
Rscript createOverlapSigMol2APA.R --file_Total "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Total.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --file_Nuclear "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Nuclear.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --output_test_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/Sig4su60QTL_overlapAPA_Total.test.chr${i}.txt" --output_test_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/Sig4su60QTL_overlapAPA_Nuclear.test.chr${i}.txt" --output_base_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/Sig4su60QTL_overlapAPA_Total.base.chr${i}.txt" --output_base_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/Sig4su60QTL_overlapAPA_Nuclear.base.chr${i}.txt"  --molPhenoQTLperm "/project2/gilad/briana/threeprimeseq/data/molecular_QTLs/perm/fastqtl_qqnorm_4su60.fixed.perm.out"
done 

run_createOverlapSigMol2APA_RNAsG.sh

#!/bin/bash


#SBATCH --job-name=run_createOverlapSigMol2APA_RNAsG
#SBATCH --account=pi-yangili1
#SBATCH --time=24:00:00
#SBATCH --output=run_createOverlapSigMol2APA_RNAsG.out
#SBATCH --error=run_createOverlapSigMol2APA_RNAsG.err
#SBATCH --partition=bigmem2
#SBATCH --mem=64G
#SBATCH --mail-type=END


module load R 
#RNAseqGeuvadis
for i in $(seq 1 22)
do
Rscript createOverlapSigMol2APA.R --file_Total "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Total.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --file_Nuclear "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Nuclear.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --output_test_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigRNAseqGeuvadisQTL_overlapAPA_Total.test.chr${i}.txt" --output_test_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigRNAseqGeuvadisQTL_overlapAPA_Nuclear.test.chr${i}.txt" --output_base_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigRNAseqGeuvadisQTL_overlapAPA_Total.base.chr${i}.txt" --output_base_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigRNAseqGeuvadisQTL_overlapAPA_Nuclear.base.chr${i}.txt"  --molPhenoQTLperm "/project2/gilad/briana/threeprimeseq/data/molecular_QTLs/perm/fastqtl_qqnorm_RNAseqGeuvadis.fixed.perm.out"
done 

run_createOverlapSigMol2APA_RNA.sh

#!/bin/bash


#SBATCH --job-name=run_createOverlapSigMol2APA_RNA
#SBATCH --account=pi-yangili1
#SBATCH --time=24:00:00
#SBATCH --output=run_createOverlapSigMol2APA_RNA.out
#SBATCH --error=run_createOverlapSigMol2APA_RNA.err
#SBATCH --partition=bigmem2
#SBATCH --mem=64G
#SBATCH --mail-type=END


module load R

#RNAseq
for i in $(seq 1 22)
do
Rscript createOverlapSigMol2APA.R --file_Total "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Total.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --file_Nuclear "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Nuclear.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --output_test_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigRNASeqQTL_overlapAPA_Total.test.chr${i}.txt" --output_test_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigRNAseqQTL_overlapAPA_Nuclear.test.chr${i}.txt" --output_base_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigRNAseqQTL_overlapAPA_Total.base.chr${i}.txt" --output_base_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigRNAseqQTL_overlapAPA_Nuclear.base.chr${i}.txt"  --molPhenoQTLperm "/project2/gilad/briana/threeprimeseq/data/molecular_QTLs/perm/fastqtl_qqnorm_RNAseq_phase2.fixed.perm.out"
done 

run_createOverlapSigMol2APA_Ribo.sh

#!/bin/bash


#SBATCH --job-name=run_createOverlapSigMol2APA_Ribo
#SBATCH --account=pi-yangili1
#SBATCH --time=24:00:00
#SBATCH --output=run_createOverlapSigMol2APA_Ribo.out
#SBATCH --error=run_createOverlapSigMol2APA_Ribo.err
#SBATCH --partition=bigmem2
#SBATCH --mem=64G
#SBATCH --mail-type=END

module load R

#Ribo
for i in $(seq 1 22)
do
Rscript createOverlapSigMol2APA.R --file_Total "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Total.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --file_Nuclear "/project2/gilad/briana/threeprimeseq/data/nominal_APAqtl_trans/filtered_APApeaks_merged_allchrom_refseqGenes.Transcript_sm_quant.Nuclear.pheno_fixed.txt.gz.qqnorm_chr${i}.nominal.out" --output_test_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigriboQTL_overlapAPA_Total.test.chr${i}.txt" --output_test_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigriboQTL_overlapAPA_Nuclear.test.chr${i}.txt" --output_base_total "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigriboQTL_overlapAPA_Total.base.chr${i}.txt" --output_base_nuclear "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigriboQTL_overlapAPA_Nuclear.base.chr${i}.txt"  --molPhenoQTLperm "/project2/gilad/briana/threeprimeseq/data/molecular_QTLs/perm/fastqtl_qqnorm_ribo_phase2.fixed.perm.out"
done 

I will need to concatinate all of the test and base files for each phenotype befre running the code to create the QQ plots.

#in base
for i in $(ls *)
do
awk '{if (NR!=1) {print}}' ${i} > ../base_nohead/${i}
done

#in test
for i in $(ls *)
do
awk '{if (NR!=1) {print}}' ${i} > ../test_nohead/${i}
done

The results are not large. I will transfer them to my computer and run the analysis here.

makeQQ=function(test, baseline, Mol, Fraction){
  names=c("chr", "start", "end", "Gene.name", "strand" ,"peaknum", "sid", "dist", "pval", "slope", "n" ,"corrPval")
  t=read.table(test,stringsAsFactors = F, col.names = names)
  t$corrPval=as.numeric(t$corrPval)
  b=read.table(baseline,stringsAsFactors = F,col.names = names)
  b$corrPval=as.numeric(b$corrPval)
  plot=qqplot(-log10(runif(nrow(b))), -log10(b$corrPval), ylab="Observed", xlab="Expected", main=paste("Overlap QTLs:", Mol, "with APA", Fraction, sep=" "))
      points(sort(-log10(runif(nrow(t)))), sort(-log10(t$corrPval)), col= alpha("Red"))
      abline(0,1)
    return(plot)
}

rna_total_plot=makeQQ("../data/mol_overlap/test/SigRNAseqQTL_overlapAPA_Total.test.txt", "../data/mol_overlap/base/SigRNAseqQTL_overlapAPA_Total.base.txt", "RNAseq", "Total")

rna_nuc_plot=makeQQ("../data/mol_overlap/test/SigRNAseqQTL_overlapAPA_Nuclear.test.txt", "../data/mol_overlap/base/SigRNAseqQTL_overlapAPA_Nuclear.base.txt", "RNAseq", "Nuclear")

rna_total_plot=makeQQ("../data/mol_overlap/test/SigRNAseqGeuvadisQTL_overlapAPA_Total.test.txt", "../data/mol_overlap/base/SigRNAseqGeuvadisQTL_overlapAPA_Total.base.txt", "RNAseq Geu", "Total")

rna_nuc_plot=makeQQ("../data/mol_overlap/test/SigRNAseqGeuvadisQTL_overlapAPA_Nuclear.test.txt", "../data/mol_overlap/base/SigRNAseqGeuvadisQTL_overlapAPA_Nuclear.base.txt", "RNAseq Geu", "Nuclear")

rna_total_plot=makeQQ("../data/mol_overlap/test/Sig4su30QTL_overlapAPA_Total.test.txt", "../data/mol_overlap/base/Sig4su30QTL_overlapAPA_Total.base.txt", "4su 30", "Total")

rna_nuc_plot=makeQQ("../data/mol_overlap/test/Sig4su30QTL_overlapAPA_Nuclear.test.txt", "../data/mol_overlap/base/Sig4su30QTL_overlapAPA_Nuclear.base.txt", "4su 30", "Nuclear")

rna_total_plot=makeQQ("../data/mol_overlap/test/Sig4su60QTL_overlapAPA_Total.test.txt", "../data/mol_overlap/base/Sig4su60QTL_overlapAPA_Total.base.txt", "4su 60", "Total")

rna_nuc_plot=makeQQ("../data/mol_overlap/test/Sig4su60QTL_overlapAPA_Nuclear.test.txt", "../data/mol_overlap/base/Sig4su60QTL_overlapAPA_Nuclear.base.txt", "4su 60", "Nuclear")

rna_total_plot=makeQQ("../data/mol_overlap/test/SigProteinQTL_overlapAPA_Total.test.txt", "../data/mol_overlap/base/SigProteinQTL_overlapAPA_Total.base.txt", "Protein", "Total")

rna_nuc_plot=makeQQ("../data/mol_overlap/test/SigProteinQTL_overlapAPA_Nuclear.test.txt", "../data/mol_overlap/base/SigProteinQTL_overlapAPA_Nuclear.base.txt", "Protein", "Nuclear")

rna_total_plot=makeQQ("../data/mol_overlap/test/SigriboQTL_overlapAPA_Total.test.txt", "../data/mol_overlap/base/SigriboQTL_overlapAPA_Total.base.txt", "Ribo", "Total")

rna_nuc_plot=makeQQ("../data/mol_overlap/test/SigriboQTL_overlapAPA_Nuclear.test.txt", "../data/mol_overlap/base/SigriboQTL_overlapAPA_Nuclear.base.txt", "Ribo", "Nuclear")

makeQQ=function(test, baseline, Mol, Fraction, plot_name){
  t=read.table(test,stringsAsFactors = F, header=T)
  b=read.table(baseline,stringsAsFactors = F,header=T)
  png(plot_name)    
  plot=qqplot(-log10(runif(nrow(b))), -log10(b$corrPval), ylab="Observed", xlab="Expected", main=paste("Overlap QTLs:", Mol, "with APA", Fraction, sep=" "))
      points(sort(-log10(runif(nrow(t)))), sort(-log10(t$corrPval)), col= alpha("Red"))
      abline(0,1)
    dev.off
}

#run function on each pheno  
makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/Sig4su30QTL_overlapAPA_Total.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/Sig4su30QTL_overlapAPA_Total.base.txt", "4su 30", "Total", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlap4su30_Total.png")
makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/Sig4su30QTL_overlapAPA_Nuclear.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/Sig4su30QTL_overlapAPA_Nuclear.base.txt", "4su 30", "Nuclear", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlap4su30_Nuclear.png")

makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/Sig4su60QTL_overlapAPA_Total.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/Sig4su60QTL_overlapAPA_Total.base.txt", "4su 60", "Total", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlap4su60_Total.png")
makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/Sig4su60QTL_overlapAPA_Nuclear.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/Sig4su60QTL_overlapAPA_Nuclear.base.txt", "4su 60", "Nuclear", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlap4su60_Nuclear.png")

makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigRNAseqGeuvadisQTL_overlapAPA_Total.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigRNAseqGeuvadisQTL_overlapAPA_Total.base.txt", "RNAseq_Guevadis", "Total", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlapRNAGue_Total.png")
makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigRNAseqGeuvadisQTL_overlapAPA_Nuclear.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigRNAseqGeuvadisQTL_overlapAPA_Nuclear.base.txt", "RNAseq_Guevadis", "Nuclear", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlapRNAGue_Nuclear.png")


makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigRNAseqQTL_overlapAPA_Total.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigRNAseqQTL_overlapAPA_Total.base.txt", "RNAseq", "Total", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlapRNA_Total.png")
makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigRNAseqQTL_overlapAPA_Nuclear.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigRNAseqQTL_overlapAPA_Nuclear.base.txt", "RNAseq", "Nuclear", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlapRNA_Nuclear.png")

makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigriboQTL_overlapAPA_Total.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigriboQTL_overlapAPA_Total.base.txt", "Ribo Seq", "Total", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlapRibo_Total.png")
makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigriboQTL_overlapAPA_Nuclear.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigriboQTL_overlapAPA_Nuclear.base.txt", "Ribo Seq", "Nuclear", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlapRibo_Nuclear.png")


makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigProteinQTL_overlapAPA_Total.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigProteinQTL_overlapAPA_Total.base.txt", "Protein", "Total", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlapProtein_Total.png")
makeQQ("/project2/gilad/briana/threeprimeseq/data/molecular_overlap/test/SigProteinQTL_overlapAPA_Nuclear.test.txt", "/project2/gilad/briana/threeprimeseq/data/molecular_overlap/base/SigProteinQTL_overlapAPA_Nuclear.base.txt", "Protein", "Nuclear", "/project2/gilad/briana/threeprimeseq/output/plots/QTL_overlap/APAoverlapProtein_Nuclear.png")

geneNames=read.table("../data/ensemble_to_genename.txt", sep="\t", header=T,stringsAsFactors = F)

genesAPA=nuclearAPA %>% separate(pid, into=c("chr", "start", "end", "id"), sep=":") %>% separate(id, into=c("Gene.name", "strand", "peaknum"), sep="_") %>% dplyr::select(Gene.name) %>% distinct(Gene.name)  %>% distinct()

su30_geneID=su30 %>% separate(pid, into=c("Gene.stable.ID", "ver"), sep ="[.]") %>% inner_join(geneNames, by="Gene.stable.ID") %>% dplyr::select("Gene.name", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval") %>% distinct()

su60_geneID=su60 %>% separate(pid, into=c("Gene.stable.ID", "ver"), sep ="[.]") %>% inner_join(geneNames, by="Gene.stable.ID") %>% dplyr::select("Gene.name", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval") %>% distinct()


rna_geneID=rna %>% separate(pid, into=c("Gene.stable.ID", "ver"), sep ="[.]") %>% inner_join(geneNames, by="Gene.stable.ID") %>% dplyr::select("Gene.name", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval") %>% distinct()


rib_geneID=rib %>% separate(pid, into=c("Gene.stable.ID", "ver"), sep ="[.]") %>% inner_join(geneNames, by="Gene.stable.ID") %>% dplyr::select("Gene.name", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval") %>% distinct()


prot_geneID=prot %>% rename("Gene.stable.ID"=pid) %>%  inner_join(geneNames, by="Gene.stable.ID") %>% dplyr::select("Gene.name", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval") %>% distinct()

Session information

sessionInfo()

R version 3.5.1 (2018-07-02)
Platform: x86_64-apple-darwin15.6.0 (64-bit)
Running under: macOS Sierra 10.12.6

Matrix products: default
BLAS: /Library/Frameworks/R.framework/Versions/3.5/Resources/lib/libRblas.0.dylib
LAPACK: /Library/Frameworks/R.framework/Versions/3.5/Resources/lib/libRlapack.dylib

locale:
[1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8

attached base packages:
[1] grid      stats     graphics  grDevices utils     datasets  methods  
[8] base     

other attached packages:
 [1] VennDiagram_1.6.20  futile.logger_1.4.3 forcats_0.3.0      
 [4] stringr_1.3.1       dplyr_0.7.6         purrr_0.2.5        
 [7] readr_1.1.1         tidyr_0.8.1         tibble_1.4.2       
[10] ggplot2_3.0.0       tidyverse_1.2.1     reshape2_1.4.3     
[13] workflowr_1.1.1    

loaded via a namespace (and not attached):
 [1] tidyselect_0.2.4     haven_1.1.2          lattice_0.20-35     
 [4] colorspace_1.3-2     htmltools_0.3.6      yaml_2.2.0          
 [7] rlang_0.2.2          R.oo_1.22.0          pillar_1.3.0        
[10] glue_1.3.0           withr_2.1.2          R.utils_2.7.0       
[13] lambda.r_1.2.3       modelr_0.1.2         readxl_1.1.0        
[16] bindrcpp_0.2.2       bindr_0.1.1          plyr_1.8.4          
[19] munsell_0.5.0        gtable_0.2.0         cellranger_1.1.0    
[22] rvest_0.3.2          R.methodsS3_1.7.1    evaluate_0.11       
[25] knitr_1.20           broom_0.5.0          Rcpp_0.12.18        
[28] formatR_1.5          backports_1.1.2      scales_1.0.0        
[31] jsonlite_1.5         hms_0.4.2            digest_0.6.16       
[34] stringi_1.2.4        rprojroot_1.3-2      cli_1.0.0           
[37] tools_3.5.1          magrittr_1.5         lazyeval_0.2.1      
[40] futile.options_1.0.1 crayon_1.3.4         whisker_0.3-2       
[43] pkgconfig_2.0.2      xml2_1.2.0           lubridate_1.7.4     
[46] assertthat_0.2.0     rmarkdown_1.10       httr_1.3.1          
[49] rstudioapi_0.7       R6_2.2.2             nlme_3.1-137        
[52] git2r_0.23.0         compiler_3.5.1